GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6351 - 6375 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0110170
  • Charcot-Marie-Tooth disease axonal type 2Q
  • Aliases:
    • CMT2Q
    • Charcot-Marie-Tooth neuropathy type 2Q
    • autosomal dominant Charcot-Marie-Tooth disease type 2Q
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q
Xenopus laevis (African clawed frog)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Drosophila melanogaster (fruit fly)
DOID:0080037
  • Worth syndrome
  • Aliases:
    • Worth's syndrome
    • autosomal dominant endosteal hyperostosis
    • autosomal dominant osteosclerosis
    • benign form of Worth hyperostosis corticalis generalisata with torus platinus
Homo sapiens (human)
DOID:0111411
  • exudative vitreoretinopathy 4
  • Aliases:
    • EVR4
Homo sapiens (human)
DOID:0110937
  • autosomal dominant osteopetrosis 1
  • Aliases:
    • OPTA1
    • autosomal dominant osteopetrosis type 1
Homo sapiens (human)
DOID:6652
  • diffuse idiopathic skeletal hyperostosis
  • Aliases:
    • Ankylosing vertebral hyperostosis
    • DISH
    • Disseminated idiopathic skeletal hyperostosis
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:0080950
  • alopecia-mental retardation syndrome 4
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Danio rerio (zebrafish)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Homo sapiens (human)
DOID:11367
  • congenital aphakia
  • Aliases:
    • APHAKIA, CONGENITAL PRIMARY
    • Congenital absence of lens
Homo sapiens (human)
DOID:0110294
  • autosomal recessive limb-girdle muscular dystrophy type 2T
  • Aliases:
    • LGMD2T
    • MDDGC14
    • muscular dystrophy limb-girdle type 2T
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
    • muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
Drosophila melanogaster (fruit fly)
DOID:0112377
  • muscular dystrophy-dystroglycanopathy type B14
  • Aliases:
    • MDDGB14
    • congenital muscular dystrophy GMPPB-related
Drosophila melanogaster (fruit fly)
DOID:0111233
  • congenital muscular dystrophy-dystroglycanopathy A14
  • Aliases:
    • MDDGA14
    • Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14
Drosophila melanogaster (fruit fly)
DOID:5530
  • thymus squamous cell carcinoma
  • Aliases:
    • Epidermoid Thymic carcinoma
Homo sapiens (human)
DOID:7926
  • epithelial malignant thymoma
  • Aliases:
    • Squamoid Thymoma
    • Thymoma, epithelial
    • Well differentiated thymic carcinoma
Homo sapiens (human)
DOID:0050579
  • glycogen storage disease XV
  • Aliases:
    • Glycogen storage disease 15
    • Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    • glycogen storage disease type XV
Danio rerio (zebrafish)
DOID:4377
  • egg allergy
  • Aliases:
    • Allergy to eggs
Homo sapiens (human)
DOID:8683
  • myeloid sarcoma
  • Aliases:
    • Chloroma
    • Extramedullary Myeloid tumor
    • Granulocytic sarcoma
Homo sapiens (human)
DOID:4330
  • non-Langerhans-cell histiocytosis
Homo sapiens (human)
DOID:5444
  • spiradenoma
  • Aliases:
    • Eccrine spiradenoma
    • Eccrine spiradenoma of skin
    • benign eccrine spiradenoma
Homo sapiens (human)
DOID:0050636
  • familial visceral amyloidosis
  • Aliases:
    • AMYLOIDOSIS, FAMILIAL RENAL
    • German type amyloidosis
    • OSTERTAG TYPE AMYLOIDOSIS
    • systemic nonneuropathic amyloidosis
Homo sapiens (human)
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Danio rerio (zebrafish)
DOID:0112275
  • developmental and epileptic encephalopathy 93
  • Aliases:
    • DEE93
    • IECEE3
    • infantile or early childhood epileptic encephalopathy 3
Xenopus tropicalis (tropical clawed frog)
DOID:0070129
  • autosomal recessive cutis laxa type IID
  • Aliases:
    • ARCL2D
Xenopus tropicalis (tropical clawed frog)

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Last updated: August 19, 2024